関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | (4-Aminophenoxy)benzene | HCID 8764 | — |
| 反応物 | 4-Amino-7-iodoquinoline | HCID 3082517 | — |
| 反応物 | 4-Chloro-7-iodoquinoline | HCID 10589540 | — |
| 溶媒 | 1-Butanol | HCID 263 | — |
| 生成物 | (4-Phenoxyphenyl)-(7-iodoquinolin-4-yl)amine | HCID 21952018 | — |
反応手順
4-Chloro-7-iodoquinoline (10 g, 34 mmol) [Semenov, V. P.; Studenikov, A. N. Synthesis of 7-iodo-4-aminoquinoline derivatives. Khim. Geterotsikl. Soedin. (1980), Issue 7, 972-5] and 4-phenoxyaniline (6.38 g, 34 mmol) in butanol (75 ml) were heated at gentle reflux (120° C.) overnight (18 hrs). On cooling the resultant precipitate was collected by filtration and washed with acetonitrile (2×50 ml). The resultant solid was suspended in chloroform (500 ml) and 2N sodium carbonate solution (300 ml) and heated at 75° C. for 45 mins. On cooling the resultant precipitate was collected by filtration, washed with water (2×50 ml) and dried to yield the product as a pale brown solid. (9.95 g, 66%) δH [2H6]DMSO 8.35(3H, m), 8.20(1H, s), 8.10(1H, d), 7.85(1H, s), 7.35(4H, m), 7.15(4H, d), 6.75(1H, d).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06713485B2 |
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| 出典データセット | uspto-grants-2004_03 |
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| ORD ID | ord-ff57ce611b9046aabc723cc98a9f5ffc |
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| 出典メモ | uspto-grants-2004_03 |
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